2019
DOI: 10.1016/j.lwt.2019.108605
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Effects of sonication during moromi fermentation on antioxidant activities of compounds in raw soy sauce

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Cited by 51 publications
(39 citation statements)
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“…The literature reports the use of the ultrasound treatment process in modifying the biological activity of peptides from various food sources. Gao et al [ 41 ] assessed the effect of sonication on the antioxidant activity of compounds in soy sauce during moromi fermentation. The authors showed that sonication increased the antioxidant properties of soy sauce, which was attributed, among others, to a significantly higher level of free amino acids and a large number of small peptides in the sonicated moromi.…”
Section: Discussionmentioning
confidence: 99%
“…The literature reports the use of the ultrasound treatment process in modifying the biological activity of peptides from various food sources. Gao et al [ 41 ] assessed the effect of sonication on the antioxidant activity of compounds in soy sauce during moromi fermentation. The authors showed that sonication increased the antioxidant properties of soy sauce, which was attributed, among others, to a significantly higher level of free amino acids and a large number of small peptides in the sonicated moromi.…”
Section: Discussionmentioning
confidence: 99%
“…Another study using Chinese-type soy sauce reported daidzin and glycitein, in addition to those mentioned before. 46 Apart from the isoflavones, other phenolic acids (e.g., vanillic acid, syringic acid, ferulic acid, and sinapic acid) have been reported in Japanese soy sauces. 47 These phenolic acids belong to the family of hydroxycinnamic and hydroxybenzoic acids, formed predominantly from the degradation of lignin during grain roasting, and during koji fermentation by Aspergillus enzymes, 48 as well as the phenylpropanoyl pathway.…”
Section: Taste-active Non-volatile Compoundsmentioning
confidence: 99%
“…Induced expression of BTWC-1 were carried out at 15°C under conditions of light irradiation (fluorescent lamp in constant-temperature shaker, 2.6 W/m 2 ) for 10 h by addition of 0.4 mM isopropyl-␤-D-thiogalactoside (IPTG) at an optical density at 600 nm (OD 600 ) of 0.5. Thereafter, 10 nM flavin adenine dinucleotide (FAD) and 10 nM flavin mononucleotide (FMN) were added and the engineering strains were cultured for another 10 h. The cells were then collected and broken by ultrasonication using the treatments and conditions listed in Table 1 (42,43). The lysed cells were resuspended in phosphate-buffered saline (PBS; NaCl 8 g/liter, Na 2 HPO 4 1.42 g/liter, KCl 0.2 g/liter, KH 2 PO 4 0.27 g/liter), followed by centrifugation at 8,000 ϫ g for 10 min to remove the cell wall fragments.…”
Section: Methodsmentioning
confidence: 99%